Evidence map›Paper›PMID 42350875›Full record

ArticleHepatology international2026

Trends in MASLD-related cirrhosis and liver cancer across diverse populations, 2010-2023.

Jialin Wu, Bonan Chen, Fuda Xie, Jiahui Hu, Mingyu Liang, Yang Lyu, Peiyao Yu, Tiejun Feng, Muyang Huang, Canbin Fang and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Hepatology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Jialin WuDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Bonan ChenDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Fuda XieDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Jiahui HuDepartment of Surgery, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.
Mingyu LiangDepartment of Obstetrics & Gynaecology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.
Yang LyuDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Peiyao YuDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Tiejun FengDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Muyang HuangDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Canbin FangDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Ka Fai ToDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Terry Cheuk-Fung YipDepartment of Medicine and Therapeutics, Medical Data Analytics Centre, The Chinese University of Hong Kong, Hong Kong, China. tcfyip@cuhk.edu.hk.
Xingxin WangShandong University of Traditional Chinese Medicine, Jinan, 250355, China. 20231000456@sdutcm.edu.cn.
Wei KangDepartment of Anatomical and Cellular Pathology, State Key Laboratory of Translational Oncology, Sir Y.K.S Pao Cancer Center, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China. weikang@cuhk.edu.hk.ORCID http://orcid.org/0000-0002-4651-677X

Funding

General Research Fund from RGC No. 14122725NSFC-RGC Joint Research Scheme N_CUHK448/23
6 · The paper itself

Abstract

BACKGROUND/

aimsMetabolic dysfunction-associated steatotic liver disease (MASLD) is now a leading cause of liver complications. This study aims to evaluate the temporal trends in the burden of MASLD-related cirrhosis and liver cancer from 2010 to 2023.

methodsUsing data from the Global Burden of Disease Study 2023, we analyzed trends in cirrhosis and liver cancer attributed to MASLD across eight selected countries. Incidence, prevalence, and mortality were analyzed and stratified by gender and age.

resultsIn 2023, China reported the highest number of MASLD-related chronic liver diseases (CLD) including cirrhosis cases, with approximately 288.64 million cases, and the highest number of liver cancer cases, at 13,780. The US recorded the highest mortality for MASLD-related CLD including cirrhosis with 6,241 deaths, while China had the highest liver cancer mortality at 9,260 deaths. From 2010-2023, trends showed significant heterogeneity. South Africa experienced the largest increase in cirrhosis prevalence (+ 52.7%), whereas South Korea was the only country with a declining incidence rate (-8.3%). The UK exhibited the most significant increase in MASLD-related liver cancer, with a 100.22% increase in prevalence and a 96.31% rise in new cases. Japan was the only country to show a decline in liver cancer burden. Generally, males bore a higher burden of MASLD-related cirrhosis and liver cancer than females, though notable exceptions existed in specific regions.

conclusionsThe burden of MASLD-related CLD including cirrhosis and liver cancer represents a significant and growing global public health challenge. Based on current trends, recommendations should prioritize improved risk stratification, early detection of advanced liver disease, and prevention targeting metabolic risk factors.

Indexed as

CirrhosisGlobal burden of diseaseLiver cancerMASLDRisk factor

Identifiers

PMID42350875

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.